services
I provide professional Quality Control documentation review and GMP compliance support with 9+ years of experience in the pharmaceutical industry.
I can assist with:
• SOP drafting and review
• Change control documentation
• Deviation documentation
• OOS/OOT review
• Audit preparation (EU audit exposure)
• QC data review
• AMV(Analytical Method Validation)
I ensure accuracy, regulatory compliance, and timely delivery.
Best for pharma companies, consultants, and regulatory teams needing structured documentation support.
Other1h
about
am a Quality Control professional with over 9 years of experience in pharmaceutical industry. I specialize in documentation review, change control, deviation handling, and regulatory compliance. I have hands-on experience with HPLC, IR Spectroscopy, and analytical instruments.
I have successfully faced EU audits and ensured full compliance with GMP guidelines. I am detail-oriented, process-driven, and committed to delivering high-quality work with accuracy and timeliness.
I can help with:
• QC documentation review
• SOP drafting & review
• Change control support
• Deviation management
• Audit preparation
• Data entry & compliance documentation
Available for remote support and consulting projects.